EP3084051A1 - Sondes d'hybridation d'acide nucléique ultra-spécifiques finement reglées - Google Patents

Sondes d'hybridation d'acide nucléique ultra-spécifiques finement reglées

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Publication number
EP3084051A1
EP3084051A1 EP14873077.3A EP14873077A EP3084051A1 EP 3084051 A1 EP3084051 A1 EP 3084051A1 EP 14873077 A EP14873077 A EP 14873077A EP 3084051 A1 EP3084051 A1 EP 3084051A1
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region
nucleic acid
expression
composition
target
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EP3084051A4 (fr
EP3084051B1 (fr
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David Yu Zhang
Juexiano WANG
Ruojia WU
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William Marsh Rice University
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William Marsh Rice University
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
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    • C07—ORGANIC CHEMISTRY
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    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
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    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
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    • C12Q1/6823—Release of bound markers
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6832—Enhancement of hybridisation reaction
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
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    • C12Q2527/00—Reactions demanding special reaction conditions
    • C12Q2527/143—Concentration of primer or probe
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    • C12Q2600/00—Oligonucleotides characterized by their use
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers

Definitions

  • these probes balance the binding energies of a target-specific "toehold" region with that of a target-nonhomologous "balance" region.
  • DNA probes have been experimentally demonstrated to function robustly to discriminate DNA targets, and RNA probes have been experimentally demonstrated to function robustly to discriminate RNA targets.
  • probes suffer from several limitations.
  • the differences in hybridization thermodynamics between nucleic acid molecules of different forms result in poor probe design, with either low specificity or low sensitivity.
  • the thermodynamic binding strength of individual base pairs/stacks are relatively large, practically precluding fine-tuning of the reaction AG 0 TM, which in turn limits the tunability of the tradeoff between probe system specificity and sensitivity.
  • published DNA and RNA hybridization thermodynamic parameters are known to be incomplete and/or inaccurate in certain conditions.
  • An in silico designed probe system may possess a real AG 0 TM that differs significantly from the calculated AG 0 TM; without a method of fine-tuning probe performance, iterative trial-and-error must be employed to achieve an optimal probe design with the desired AG 0 TM.
  • the present disclosure provides, according to certain instances, highly specific nucleic acid hybridization probe systems, which reliably discriminate single-base changes in target nucleic acids.
  • the probe systems described in the present disclosure excel in (1) reliably probing DNA, RNA, and modified nucleic acid targets with DNA, RNA, and other nucleic acid probes, and (2) enabling fine- tuning of the tradeoff between sensitivity and specificity.
  • the compositions and methods of the present disclosure may be useful in, among other things, molecular cancer diagnostics, infectious disease diagnostics, food safety diagnostics, and research discovery tools based on DNA and RNA detection and quantification.
  • a composition for selective interaction with a target nucleic acid molecule comprises a first concentration of a first nucleic acid strand comprising a first region, second region, and third region, and a second concentration of a second nucleic acid strand comprising a fourth region and fifth region.
  • the target nucleic acid comprises a sixth and seventh region of a nucleotide sequence that is at least partially, if not fully, complementary to a nucleotide sequence of the first and second regions, respectively.
  • the AG° t -Tc term of Expression 1 represents the standard free energy of hybridization between the sixth region and the first region; the AG° n -pc term of Expression 1 represents the free energy of hybridization between the fifth region and the third region; the AG° V _ T C term of Expression 1 represents the standard free energy of hybridization between the seventh region and the second region; and the AG P C term of Expression 1 represents the standard free energy of hybridization between the fourth region and the second region.
  • the method of calculating AG° values is described in detail later in the description.
  • the concentration of the target nucleic acid is smaller than the first concentration. In certain other instances, the concentration of the target nucleic acid is equal to or greater than the first concentration.
  • the target nucleic acid further comprises an eighth region adjacent to the seventh region, such that the eighth region nucleotide sequence is not complementary to the third region nucleotide sequence, with fewer than 50% of the aligned nucleotides paired between the eighth and the third region at equilibrium.
  • a process for creating a nucleic acid probe comprises the following steps: selecting a target nucleotide sequence in a nucleic acid molecule, the target nucleotide sequence comprising a sixth nucleotide subsequence and a seventh nucleotide subsequence; selecting a first nucleotide sequence comprising a first nucleotide subsequence, a second nucleotide subsequence, and a third nucleotide subsequence; and selecting a second nucleotide sequence comprising a fourth nucleotide subsequence and a fifth nucleotide subsequence.
  • the process further comprises the step of synthesizing a first nucleotide strand comprising the first nucleotide sequence and a second nucle
  • the process may alternatively or further comprise selecting the first and second concentrations such that the standard free energy as determined by Expression 2 (-Rrin(([P] 0 - [C] 0 )/[C] 0 )) is within 5 kcal/mol of the standard free energy as determined by Expression 1 (AG 0 TM) where the terms [C]o and [P]o of Expression 2 represent a predetermined concentration of the first nucleotide strand and the second nucleotide strand, respectively, R equals the universal gas constant 8.314 J/mol » K, and ⁇ equals the temperature in Kelvin.
  • the predetermined concentration of at least one of the first nucleic acid strand or the second nucleic acid strand may be modified until this condition is met.
  • optimization may occur by repeating the steps of the process and selecting modified nucleotide sequences that meet the desired free energy conditions.
  • a method for identifying the presence or quantity of a nucleic acid molecule bearing the target nucleotide sequence in a sample comprises applying a probe to a sample possibly comprising a target nucleic acid molecule and operating the hybridization reaction at a temperature from about 4°C to about 75°C, from about 25°C to about 70°C, or from about 37°C to about 65°C, or any temperature range there between, to permit hybridization of the probe to the target nucleic acid molecule, if the target nucleic acid molecule is present in the sample.
  • the probe comprises a first nucleic acid strand and a second nucleic acid strand.
  • the first nucleic acid strand comprises a first region, a second region, and a third region, wherein the first region possesses a nucleotide sequence that is complementary to a nucleotide sequence of a sixth region of the target nucleic acid molecule, and wherein the second region possesses a nucleotide sequence that is complementary to a nucleotide sequence of a seventh region of the target nucleic acid molecule.
  • the second nucleic acid strand comprising a fourth region and a fifth region, wherein the fourth region possesses a nucleotide sequence that is complementary to the nucleotide sequence of the second region, and wherein the fifth region possesses a nucleotide sequence that is complementary to the nucleotide sequence of the third region.
  • the target nucleic acid molecule is R A.
  • a method for selectively amplifying a target nucleic acid sequence from a sample comprising applying the probe as an enzymatic primer to a mixture comprising the sample, a DNA or RNA polymerase, and a mixture of nucleotide triphosphates.
  • the mixture further comprises an additional DNA or RNA primer, or an additional enzyme, such as a nicking enzyme, a recombinase, a helicase, a restriction enzyme, a nuclease, or a ligase.
  • the combination of the probe and the mixture are allowed to react isothermally for between 1 minute and 72 hours. In some instances, the combination of the probe and the mixture are allowed to react through a number of temperature cycles, varying between 5 and 200 cycles.
  • FIG. 1 provides one embodiment of a suitable nucleic acid probe system 10 for use in the present invention.
  • Probe system 10 comprises a complement strand C (also referred to herein as the "first strand” and a protector strand P (also referred to herein as the "second strand") designed with respect to a target nucleic acid T (also referred to as “target nucleic acid molecule,” or “target nucleic acid strand”).
  • Complement strand C includes a target-toehold- complementary region 1 (also referred to herein as the "first region”), a target-homologous complementary region 2 (also referred to herein as the "second region”), and a target- nonhomologous-complementary region 3 (also referred to herein as the "third region”).
  • the protector comprises a target-homologous region 4 (also referred to herein as the "fourth region”) and a target-nonhomologous region 5 (also referred to herein as the "fifth region”).
  • the target comprises a target-toehold region 6 (also referred to herein as the "sixth region") and a target- validation region 7 (also referred to herein as the "seventh region”).
  • the target may further comprise a target upstream region 8, and/or additional unnamed upstream and downstream regions.
  • the target homologous region 4 of protector P may differ in sequence from the target validation region 7 of target T, for example in the instance protector P and target T are different types of nucleic acids (e.g., RNA vs. DNA).
  • region when referring to the probe system or target nucleic acid defines a group of contiguous nucleotide bases that act as a functional unit in hybridization and dissociation.
  • FIG. 2 A provides an exemplary probe system 10 and its reaction with target nucleic acid T and FIG. 2B provides and exemplary probe system 10 and its reaction with a variant target V having a single-base difference 12 than target T in the target validation region 7.
  • probe system 10 is designed such that the standard free energy of the hybridization reaction of probe system 10 with intended target T (AG 0 TM, ) is approximately equal to (-Rrin(([P] 0 - [C]o)/[C]o)) (Expression 2), and ensures a medium to high yield of complement strand C bound to target T.
  • AG°v AG 0 rxn + AAGV NP
  • AAGV NP denotes the relative thermodynamic penalty of the single base change.
  • FIG. 3 provides the various standard free energies of the binding region components that are used in the present invention to calculate the reaction standard free energy (AG 0 TM,).
  • FIG. 4 provides a distribution of (AGV T C - AGV P C ) values for 46 different 50 nt non-overlapping subsequences of BRAF expressed (exonic) mRNA at different temperatures, assuming that the first nucleic acid molecule and second nucleic acid molecules are both DNA.
  • AGV T C - AGV P C a distribution of (AGV T C - AGV P C ) values for 46 different 50 nt non-overlapping subsequences of BRAF expressed (exonic) mRNA at different temperatures, assuming that the first nucleic acid molecule and second nucleic acid molecules are both DNA.
  • AG T C - AGV P C the results here demonstrate that the AG T C - AGV P C term should be considered in the design of the probes described herein and thereby improves upon prior art design parameters.
  • the label of protector strand P is a quencher Q that is specific to fluorophore F of complement strand C.
  • FIG.6 is a representation of one aspect of the present method for tuning probe system behavior. Specifically, in addition to modulation of reaction standard free energy (AG 0 TM) via addition or removal of base stacks (modification of value of Expression 1), modulation of stoichiometry (ratio of the concentrations of P to C) can be utilized to control the tradeoff between specificity and sensitivity of the probe and provides a more effective method of doing so (modifying the value of Expression 2).
  • Modulating P to C stoichiometry is also beneficial when AG 0 TM cannot be accurately calculated in silico by allowing rescue of probe systems with real AG 0 TM that differs by up to 5 kcal/mol from their calculated AG 0 TM.
  • FIG. 7 represents variant probe system designs.
  • FIG. 7A represents a probe system with opposite 573 ' orientation.
  • FIG. 7B represents a probe system in which region 1 is embedded within region 2, or in which region 1 exists between regions 2 and 3.
  • FIG. 7C represents a probe system in which regions 2 and 4 are not perfectly complementary, or in which regions 3 and 5 are not perfectly complementary.
  • FIG. 8 provides a graphical representation of the different desired yield for target binding, and the tradeoff between specificity and sensitivity. If the reaction standard free energy AG 0 TM as determined by Expression 1 (or Expression 3 if a label is used) deviates from (Expression 2 or -Rxln(([P] 0 - [C]o)/[C]o)]) by free energy deviation X, the yield of the target binding will likewise change. For positive values of X, the specificity (against a target variant V) will be improved, but sensitivity (yield) will be reduced. For negative values of X, the sensitivity will be improved, but specificity will be reduced. For particular applications, either specificity or sensitivity may be more important, and the ability to fine-tune thermodynamics via methods presented herein improves upon the prior art.
  • X +1.42 kcal/mol
  • X is -1.27 kcal/mol.
  • FIG. 21 provides a schematic overview of hotspot multiplexing PCR using probes of the present disclosure as primers.
  • a sample 20 that comprises desired target nucleic acid molecules 22 is mixed with enzyme 23, a forward primer 24, and a reverser primer set 10a- lOd.
  • the target nucleic acid molecules 22 comprise single-base mutations residing at loci close to one another (a "hotspot"), and are typically challenging to detect via standard PCR primers. Due to the fact that the present probes possess selectivity to single nucleotide mismatches along the entire length of the primer, the present probes may be uniquely advantageous in hotspot multiplexed PCR primers.
  • FIG. 23 provides fine-tuning of probes directed to a DNA target by modifying the [P]o/[C]o ratio.
  • Probes in this figure were designed to bind to the same DNA target with different reaction standard free energies.
  • Each complement strand was modified by a TAMRA fluorophore at 3' end while each protector strand by an Iowa Black RQ quencher at 5' end.
  • Hybridization yields were experimentally obtained at different ([P] 0 - [C] 0 )/[C] 0 ratios via fluorescence. The results indicate that each probe shown in this figure is tunable in specificity and sensitivity. All experiments were done with IX PBS at 25 °C.
  • FIG. 24 provides fine-tuning of probes targeting an RNA sequence (synthetic miPv-122) by modifying the[P]o/[C]o ratio.
  • the probe design process was similar to that of Fig. 22, except that RNA-DNA binding parameters were used. Experimental procedures were the same as DNA target. The results show that the sensitivity/specificity tradeoff of probes for RNA target are also adjustable.
  • FIG. 25 provides a schematic overview of selectively amplifying a target nucleic acid molecule using probes of the present disclosure as self-reporting primers.
  • the first nucleic acid strand of the primer 10 comprises a fluorophore F on one end
  • the second nucleic acid strand of the primer comprises a quencher Q on the other end.
  • fluorescence signal increases as the second nucleic acid strand of the primer P diffuses away, indicating the formation of amplicon 26.
  • FIG. 26 provides a schematic overview of amplifying a target nucleic acid molecule using probes of the present disclosure as fluorophore-labeled probes to quantitate the amount of desired amplicons formed through the amplification.
  • a sample that possibly comprises desired target nucleic acid molecule 22 is mixed with enzyme 23, forward primer 27, reverse primer (not shown), and fluorophore-labeled probe 10.
  • the first nucleic acid strand of the probe C is functionalized with a fluorophore F internally and a quencher at the 3 ' end, so that the probe is natively dark due to the close proximity of the fluorophore and quencher.
  • the forward primer and the first nucleic acid strand of the probe C hybridize to the desired target nucleotide molecule during the annealing process 31 , while the second nucleic acid strand is displaced by the target nucleic acid molecule.
  • enzyme 23 with exonuclease activity extends the primer and cleaves the phosphodiester bonds of first nucleic acid strand, resulting the increase of fluorescence signal.
  • the nucleic acid probe systems described herein possess provide several advantages over previously described system.
  • First, the methods and compositions described herein provide for more economical DNA probes to assay RNA targets of specific sequence; DNA probes to RNA targets may also exhibit improved specificity because RNA hybridization is generally less specific than DNA hybridization. Additionally, the methods and compositions here allow modified nucleic acid probes, such as those incorporating 2'-0-methyl nucleotides or locked nucleic acid (LNA), to benefit from robust single nucleotide specificity; these modified nucleic acid probes may possess desirable properties such as nuclease resistance. Second, the methods and compositions described herein provide specificity and sensitivity performance which can be finely tuned by modification of the relative concentrations of protector and complement in the probe system.
  • LNA locked nucleic acid
  • the probe systems also possess two other desirable features: the probes described herein are extremely specific and the probes described herein are operable across a wide range of temperature and salt concentrations and are therefore functionally reliable under many different experimental conditions. For example, a single-base change results in binding yields that differ by approximately 30-fold across temperatures from 10°C to 70°C. Finally, the probes described herein are kinetically fast. For example, the probe of the present disclosure interacts with the target nucleic acid molecule within a factor of 10 of hybridization.
  • probe system 10 consists of a protector oligonucleotide/strand P and a complement oligonucleotide/strand C with the protector P existing in excess of the complement C.
  • Protector P and complement C can hybridize to form a partially double-stranded complex; this is true regardless of whether protector P and complement C are introduced separately to target T, or pre-reacted to form the complex.
  • there may be an excess of complement C or protector P such that the excess strand may exist as a single stranded molecule in addition to the partially double stranded complex of protector and complement.
  • the concentration ratio [P]o / [C]o is selected so that the reaction between target T and probe system 10 has a reaction standard free energy (AG 0 TM) equal to (-Rrin(([P] 0 - [C]o)/[C]o)]).
  • AG 0 TM reaction standard free energy
  • FIG. 2B a target variant V that differs in sequence from target T in the target- validation 7 or target-toehold 6 regions, potentially by a single base, will bind with more a positive standard free energy (AG°v) and possess significantly lower equilibrium yield (e.g. 2%).
  • the sequences of protector strand P and complementary strand C are designed based on the sequence of intended target T. Each strand is conceptually divided into a number of non-overlapping regions, as shown in FIG. 1. It is important to note that target- validation region 7 (also referred to herein as the "seventh region”) and target-homologous region 4 (also referred to herein as the "fourth region”), while both are partially or fully complementary to target- homologous-complementary region 2 (also referred to herein as the "second region”), can possess different sequences.
  • an RNA target will have a target- validation region 7 containing uracil whereas a DNA protector P will comprise thymine in target-homologous region 4.
  • region 4 may be partially mismatched to region 2 at certain positions, whereas region 7 is perfectly matched to region 2.
  • both region 4 and region 7 may be partially mismatched to region 2, but at different nucleotide bases.
  • Expressions 1 and 3 are comprised of a number of components representing the standard free energy of hybridization between the various regions of the protector/complementary/target nucleic acid strands.
  • the AG° t - T c term represents the standard free energy of hybridization between target-toehold region 6 of target nucleic acid T and target-toehold complementary region 1 of complement strand C of probe system 10.
  • These regions can be either partially complementary or fully complementary.
  • the term “partially complementary” is defined as having over 60% of the nucleotides in the first region being complementary to the aligned nucleotides of the sixth region.
  • the term “partially complementary” with respect to other paired sequences may have a different meaning.
  • the AG°nh-pc term represents the standard free energy of hybridization between target-nonhomologous region 5 of protector strand P and target-nonhomologous-complementary region 3 of complement strand C. These regions can be either partially complementary or fully complementary. In this instance, the term “partially complementary” is defined as having over 60% of the nucleotides in the third region being complementary to the aligned nucleotides of the fifth region.
  • the AG° V _TC term represents the standard free energy of hybridization between target-validation region 7 of target nucleic acid T and target-homologous-complementary region 2 of complement strand C. These regions can be either partially complementary or fully complementary. In this instance, the term “partially complementary” is defined as having over 60% of the nucleotides in the second region being complementary to the aligned nucleotides of the seventh region.
  • the AG°h-pc term represents the standard free energy of hybridization between the target-homologous region 4 of protector strand P and target-homologous-complementary region 2 of complement strand C. These regions can be either partially complementary or fully complementary. In this instance, the term “partially complementary” is defined as having over 60% of the nucleotides in the second region being complementary to the aligned nucleotides of the fourth region.
  • “little to no secondary structure” in the target-toehold-complementary region is defined as fewer than 50% of the nucleotides in the region being in double-stranded state in the evaluated minimum free energy structure, as computed in the operational temperature and salinity conditions.
  • “little to no binding" between the target-upstream region and target-nonhomologous-complementary region 3 is defined as fewer than 50% of the nucleotides in the target-nonhomologous-complementary region 3 being in double-stranded state in the evaluated minimum free energy structure, as computed in the operational temperature and salinity conditions.
  • the present probe design includes consideration of the relative concentrations of the protector and complement strands of the probe. This permits fine tuning of reactions by modifying the ratio of protector strand to complement strand independently of the probe's sequence design.
  • the design of the present nucleic acid hybridization probe system is based on the following:
  • X is a value between -5 kcal/mol and +5 kcal/mol.
  • the value of X further allows the user to control the tradeoff between high molecular sensitivity and high molecular specificity, with more positive values of X favoring higher specificity.
  • WO 2012/058488 describes the design of nucleic acid hybridization probes in which the primary design constraint is AGVrc ⁇ AG 0 n h-pc, in the language of the present disclosure, where approximately equal to is defined as within 10% of each other.
  • the standard free energies AG° t _Tc and for the probes of the current invention differ by more than 10% because the desired value of X differs significantly from 0.
  • the standard free energies AG° t -Tc and AG° n h-pc for the probes of the current invention differ by more than 10% because (AGV T C - AGV P C) differs significantly from 0.
  • the standard free energies AG° t _Tc and AG° n -pc for the probes of the current invention differ by more than 10%> because ([P]o - [C]o)/[C]o differs significantly from 1.
  • the standard free energies AG° t -Tc and AG° n h-pc for the probes of the current invention differ by more than 10% because AG°i abe i differs significantly from 0.
  • the present probe system diverges from the prior art in the consideration of the AGV T C, AGV P C, AG beh X, and 1 1 € 3 ⁇ 4 ' terms.
  • Negligence of the AGV T C, AGV P C terms lead to poor probe design in many settings where the nucleotide sequences of region 4 and region 7 are not identical
  • negligence of the AGV be i term leads to poor probe design when fluorophore or other labels are used
  • negligence of the X term precludes different tradeoffs between specificity and sensitivity
  • negligence of the stoichiometric ratio term precludes fine- tuning of probe system behavior independent of sequence design and furthermore cause probes to perform poorly in certain stoichiometries of P and C.
  • the target- validation region 7 of the target T and target-homologous region 4 of protector P may differ in sequence and thermodynamic properties for a number of reasons, importantly in instances where T and P are different types of nucleic acids.
  • target T may be an RNA molecule due to scientific/clinical interest
  • protector P may be a DNA molecule due to economics/synthesis capabilities.
  • protector P may comprise a modified nucleic acid, such as 2'-0-methyl nucleotides or locked nucleic acid (LNA).
  • region 4 and region 7 may both be DNA, but differ in nucleotide sequence in order to benefit from increased kinetics or decreased unwanted biological response.
  • RNA targets T using DNA probes is only one application in which AGV T C - AGV P C must be considered.
  • Other variations of the probe system exist where the target-homologous region of protector P differs from the target-validation region of the target T, either because T and P are different types of nucleic acids (RNA, DNA, LNA, PNA, phosphothioate DNA, 2'-methoxy nucleic acids, etc.) or because of small changes in sequence, which will be discussed in further detail herein below.
  • labels can be organic fluorophores, metallic nanoparticles, or haptens that recruit antibodies. Frequently, these labels can have significant thermodynamic effects, stabilizing or destabilizing nucleic acid hybridization. Proper design of probe systems that utilize labels should account for the differential standard free energies of labels with the protector and with the target as shown in FIG. 5.
  • the targets biological DNA or RNA molecules
  • P and PC concentrations of P and PC
  • [ TCL ) yield or sensitivity of the probe system to target T, which can be expressed as " [T] TC] >
  • [T] TC] >
  • the fold-change discrimination against a variant target V [TC]/[VC]) is within a factor of 2 of optimal.
  • the standard free energy of a reaction can be related to the reaction equilibrium constant by the following expression.
  • [P]o denotes the initial concentration of the protector and [C]o denotes the initial concentration of the complement.
  • the equilibrium concentrations of [P] and [PC] can be approximated as [P]o - [C]o and [C]o, respectively.
  • the term is scale-invariant, and the concentrations used for [P]o and [C]o can therefore be either the high stock concentration added to a sample, or the final concentration achieved after dilution by the sample.
  • [P]o and [C]o refer to the total concentrations of P and C, including those present in the partially double-stranded PC species.
  • An alternative method of writing this expression is ([P free ]o / [PC] 0 ), where [P free ]o denotes the initial concentration of free P and [PC]o denotes the initial concentration of PC.
  • the concentration for [P]o may be lower than, the same as, or greater than, but is generally greater than the concentration for [C]o.
  • the concentration for [P] 0 as can be from about 1.01 times to about 10,000 times that of [C]o, from about 1.1 times to about 1 ,000 times that of [C]o, or from about 1.2 times to about 100 times that of [C]o and including any intermediate range between any of the above provided ranges.
  • probe behavior can be tuned to achieve approximately 50% sensitivity by designing the probe system so that the AG 0 TM is close to 0, or from about -5 kcal/mol to about +5 kcal/mol, and then adjusting the [P]o and [C]o so that
  • FIG. 6 demonstrates that a single additional base pair changes the value of AG 0 TM by between -0.6 kcal/mol and -2.2 kcal/mol in 37 °C, 1M Na + .
  • thermodynamics via P to C stoichiometry is over a factor of 50 more fine-grained than prior art methods of tuning thermodynamics via additional base pairs (-0.012 kcal/mol vs -0.60 kcal/mol).
  • Tuning of P and C stoichiometry can occur at the design phase, or dynamically as the probe is being iteratively optimized for a particular application.
  • FIGS. 22 and 23 demonstrate the effectiveness of adjusting the ratio ([P]ofind-[C]o)/[C]o in order to tune the specificity/sensitivity tradeoff.
  • Fig. 22 depicts the sequence design of four different probes directed to a DNA target, each designed with a different AG 0 TM and the observed yield of the DNA target to each probe for different values of ([P]o-[C]o)/[C]o.
  • FIG. 23 depicts the sequence design of five different probes directed to a RNA target, each designed with a different AG 0 TM and the observed yield of the RNA target to each probe for different values of ([P]o 0 -[C]o)/[C] 0 .
  • larger values of ([P]o-[C]o)/[C]o monotonically decrease the yield of the hybridization between the target and the probe.
  • the present disclosure provides a probe system in which
  • thermodynamic property of the present probe system can be expressed by the following:
  • X is the deviation from 0.
  • the value of X is from about -5 kcal/mol to about +5 kcal/mol.
  • the specificity (against a target variant V) will be improved, but sensitivity (yield) will be reduced.
  • the sensitivity will be improved but specificity will be reduced as demonstrated in FIG. 8.
  • certain applications (such as those dealing with rare alleles) may require higher specificity at the cost of sensitivity, or vice versa.
  • the present methods to fine-tune thermodynamics are particularly useful for these applications that require intricate control of sensitivity and specificity (see also Variants).
  • the present disclosure provides for minor sequence differences between target-validation and target-homologous regions.
  • the target-validation region (of the target T) and the target-homologous region (of the protector P) are both intended to be complementary to the target-homologous-complementary region (of the complement C).
  • the target-validation and/or the target-homologous region are only partially complementary to the target-homologous- complementary region.
  • the resulting probes maintain consistency with the principles of probe construction described herein.
  • the present disclosure provides a probe system in which the 5 ' to 3 ' orientations of the protector and complement are reversed with respect to the positions of the nonhomologous and toehold regions as shown in FIG. 7.
  • Modern nucleic acid synthesis occurs from the 3' end to the 5' end, resulting in truncations and deletions being concentrated at the 5' end. Consequently, it is expected that the original orientation shown in FIGS. 1-6 would be desirable because truncations on the protector and the complement will tend to balance each other energetically, maintaining the desired AG 0 TM.
  • FIG. 7 In contrast, in the design orientation shown in FIG.
  • the reaction AG 0 ⁇ is broken down into the sum of a number of AG 0 terms denoting the standard free energy of hybridization of various regions of the complement strand to target strand and complement strand to protector strand (e.g. AG - P C denotes the hybridization of the target-nonhomologous region to the target- nonhomologous-complement region).
  • AG - P C denotes the hybridization of the target-nonhomologous region to the target- nonhomologous-complement region.
  • the values of these terms can be approximately calculated by adding the standard free energies of base stacks as described in more detail herein below, though current literature -provided standard free energy values are incomplete and of limited accuracy.
  • Experimental testing is needed to determine the true values of AG 0 TM for each probe, but the literature-guided values provide a rough (typically within 3 kcal/mol or 15%) estimate of the AG 0 TM,.
  • the standard free energies of hybridization between regions of the present probe system are calculated based on a base pair stacking approach.
  • two adjacent base pairs comprise one stack, which has a defined enthalpy ( ⁇ 0 ) and entropy (AS 0 ) value.
  • the standard free energies of several stacks can be summed to evaluate the standard free energy of a binding region.
  • the standard free energy of a 'CTC region pairing to a 'GAG' region is the standard free energy of stack 'CT/GA' plus the standard free energy of stack 'TC/AG'.
  • the standard free energy of stack 'CT/GA' is -1.28 kcal/mol and the standard free energy of stack 'TC/AG' is -1.30 kcal/mol, so the standard free energy of 'CTC pairing to 'GAG' is -2.58 kcal/mol.
  • the AS 0 of base stacks are adjusted by 0.368 * ln([Na + ]) cal/mol*K, regardless of nucleotide base identity, due to the electrostatic screening properties of cations.
  • divalent cations such as Mg 2+
  • denaturants such as formamide may be used to facilitate hybridization reactions, particularly for in situ hybridization applications. It has been reported in literature that each percent (%) that water is replaced by formamide effectively increases the temperature by 0.6°C for purposes of nucleic acid base pairing thermodynamics, see Blake and Delcourt, Nucleic Acids Research, 1996.
  • reaction standard free energy AG 0 TM from Expression 1 or 3
  • AG°t_TC hybridization of target-toehold-region (region 6) to target-toehold- complementary regions (region 1)
  • AG°ini initiation energy penalty
  • the probes described herein have a AG° t - T c from about -2 kcal/mol to about -16 kcal/mol, from about -5 kcal/mol to about -13 kcal/mol, or from about -7 kcal/mol to about -10 kcal/mol at operation conditions.
  • AG° nh -pc hybridization of target-nonhomologous region 5 of protector P to target- nonhomologous-complementary region 3 of complement C
  • AGVi hybridization initiation energy
  • the sum of the standard free energy of hybridization between the target-toehold-complementary region (region 1) and the target-toehold region (region 6) and between the target-homologous-complementary region (region 2) and the target-validation region (region 7) is more negative than -7 kcal/mol, for example between about -7 kcal/mol and about -70 kcal/mol, between about -7 kcal/mol and about -50 kcal/mol, and between -7 kcal/mol and about -30 kcal/mol.
  • the sum of the standard free energy of hybridization between the target-nonhomologous-complementary region (region 3) and the target-nonhomologous region (region 5) and between the target- homologous region (region 4) and the target-homologous-complementary region (region 2) is more negative than -10 kcal/mol, for example between about -10 kcal/mol and about -70 kcal/mol, between about -10 kcal/mol and about -50 kcal/mol, and between -10 kcal/mol and about -30 kcal/mol.
  • the probes of the present disclosure are useful in PCR application or other isothermal amplification systems as primer, for example, in hotspot multiplexing PCR reactions.
  • primers for example, in hotspot multiplexing PCR reactions.
  • two or more primer systems for non-identical targets can be combined into one solution for hotspot multiplexing PCR.
  • a schematic of hotspot multiplexing PCR is shown in Fig. 21.
  • the sequences of targets in one multiplexing group can be highly similar due to the high specificity characteristic of the primer system.
  • the design process for each primer system in the primer set is the same as that of the probes as described above. The specificity and sensitivity of each primer system could be adjusted according to experimental results.
  • An example of primer systems for hotspot multiplexing PCR is shown in FIG. 22.
  • the signal generation method for PCR or other isothermal amplification systems is using fluorophore-modified complement and quencher-modified protector.
  • the protector would detach from the complement as the amplification proceeds, so the fluorescence signal is proportional to the copy number of amplified target. Different targets can be quantitated simultaneously by using spectral non-overlapping fluorophores.
  • a similar signal generation method is using fluorophore-modified complement and quencher-modified protector as self-reporting primers as shown in FIG. 25.
  • Another signal generation method that similar to traditional TaqMan probes is using fluorophore- and quencher-modified complement and non- modified protector as detection probes as shown in FIG. 26.
  • probes that bear different fluorophores can be used for different desired targets.
  • the TaqMan-like probes presented in this disclosure may be uniquely advantageous in distinguishing similar targets.
  • Each probe system described herein may be comprised of DNA, RNA, or analogs thereof, and/or combinations thereof.
  • a probe system comprises one or more non-natural nucleotides.
  • the incorporation of non-natural nucleotides in the primers can further augment the performance of the probe systems, such as by providing improved per-base binding affinity and increased nuclease resistance.
  • probe systems described herein may also be applied in the context of initiating enzymatic reactions; in such uses, the probe systems are referred to as primer systems, though the composition and method of action remains the same.
  • primer systems as described in this disclosure possess high specificity and capability for fine-tuning of performance, offering advantages to enzymatic assays of nucleic acids.
  • the primers described herein serve as starting points for polymerase extensions, including but not limited to polymerase chain reaction for replication of DNA templates, transcription for production of RNA from DNA templates, and reverse transcription for production of DNA from RNA templates, isothermal DNA and RNA amplification methods such as Nucleic Acid Sequence Based Amplification (NASBA), Loop mediated isothermal Amplification (LAMP), Helicase-Dependent Amplification (HDA), Recombinase Polymerase Amplification (RPA), isothermal Exponential Amplification Reaction (EXPAR), Nicking Enzyme Amplification Reaction (NEAR), Rolling Circle Amplification (RCA), and Transcription Mediated Amplification (TMA).
  • NASBA Nucleic Acid Sequence Based Amplification
  • LAMP Loop mediated isothermal Amplification
  • HDA Helicase-Dependent Amplification
  • RPA Recombinase Polymerase Amplification
  • EXPAR isothermal Exponential Amplification Reaction
  • NEAR Nicking Enzyme Amplification Reaction
  • a "target” for a probe system described herein can be any single-stranded nucleic acid, such as single-stranded DNA and single-stranded RNA, including double-stranded DNA and RNA rendered single-stranded through heat shock, asymmetric amplification, competitive binding, and other methods standard to the art.
  • a "target” for a primer system can be any single- stranded (ss) or double- stranded (ds) nucleic acid, for example, DNA, RNA, or the DNA product of RNA subjected to reverse transcription. In some instances, a target may be a mixture (chimera) of DNA and RNA.
  • a target comprises artificial nucleic acid analogs, for example, peptide nucleic acids (Nielsen et al. Science 254(5037): 1497-500 (1991)) or locked nucleic acids (Alexei et al. Tetrahedron 54(14): 3607-30 (1998)).
  • a target may be naturally occurring (e.g., genomic DNA) or it may be synthetic (e.g., from a genomic library).
  • a "naturally occurring" nucleic acid sequence is a sequence that is present in nucleic acid molecules of organisms or viruses that exist in nature in the absence of human intervention.
  • a target is genomic DNA, messenger RNA, ribosomal RNA, micro-RNA, pre-micro-RNA, pro-micro-RNA, long non-coding RNA, small RNA, epigenetically modified DNA, epigenetically modified RNA, viral DNA, viral RNA or piwi-RNA.
  • a target nucleic acid is a nucleic acid that naturally occurs in an organism or virus.
  • a target nucleic is the nucleic acid of a pathogenic organism or virus.
  • the presence or absence of a target nucleic acid in a subject is indicative that the subject has a disease or disorder or is predisposed to acquire a disease or disorder.
  • the presence or absence of a target nucleic acid in a subject is indicative that the subject will respond well or poorly to a treatment, such as a drug, to treat a disease or disorder.
  • a treatment such as a drug
  • the presence or absence of a target nucleic acid in a subject is indicative that the subject who has been treated previously for cancer and is in remission may be at risk of cancer recurrence.
  • polynucleotide refers to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Polynucleotides may have any three-dimensional structure, and may perform any function.
  • polynucleotides coding or non-coding regions of a gene or gene fragment, loci (locus) defined from linkage analysis, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers.
  • a polynucleotide may comprise modified nucleotides, such as methylated nucleotides and nucleotide analogs.
  • modifications to the nucleotide structure may be imparted before or after assembly of the polymer.
  • a polynucleotide may be further modified, such as by conjugation with a labeling component.
  • the term "recombinant" polynucleotide means a polynucleotide of genomic, cDNA, semi- synthetic, or synthetic origin which either does not occur in nature or is linked to another polynucleotide in a non-natural arrangement.
  • isolated nucleic acid refers to a polynucleotide of natural or synthetic origin or some combination thereof, which (1) is not associated with the cell in which the "isolated nucleic acid” is found in nature, and/or (2) is operably linked to a polynucleotide to which it is not linked in nature.
  • a nucleic acid may also encompass single- and double- stranded DNA and RNA, as well as any and all forms of alternative nucleic acid containing modified bases, sugars, and backbones.
  • nucleic acid thus will be understood to include, but not be limited to, single- or double- stranded DNA or RNA (and forms thereof that can be partially single- stranded or partially double- stranded), cDNA, aptamers, peptide nucleic acids ("PNA"), 2 '-5' DNA (a synthetic material with a shortened backbone that has a base- spacing that matches the A conformation of DNA; 2 '-5' DNA will not normally hybridize with DNA in the B form, but it will hybridize readily with RNA), and locked nucleic acids (“LNA”).
  • Nucleic acid analogues include known analogues of natural nucleotides that have similar or improved binding, hybridization of base -pairing properties.
  • Analogous forms of purines and pyrimidines are well known in the art, and include, but are not limited to aziridinylcytosine, 4-acetylcytosine, 5- fluorouracil, 5-bromouracil, 5-carboxymethylaminomethyl-2-thiouracil, 5- carboxymethylaminomethyluracil, inosine, N6-isopentenyladenine, 1-methyladenine, 1- methylpseudouracil, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N.sup.6-methyladenine, 7- methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D- mannosylqueosine, 5-methoxyuracil, 2-methylthio- N6-isopentenyladenine, uracil
  • DNA backbone analogues provided herein include phosphodiester, phosphorothioate, phosphorodithioate, methylphosphonate, phosphoramidate, alkyl phosphotriester, sulfamate, 3'-thioacetal, methylene(methylimino), 3'-N-carbamate, morpholino carbamate, and peptide nucleic acids (PNAs), methylphosphonate linkages or alternating methylphosphonate and phosphodiester linkages (Strauss-Soukup, 1997, Biochemistry 36:8692-8698), and benzylphosphonate linkages, as discussed in U.S. Pat. No.
  • nucleic acids herein can be extracted from cells or synthetically prepared according to any means known to those skilled in the art; for example, the nucleic acids can be chemically synthesized or transcribed or reverse transcribed from cDNA or m NA, among other sources.
  • a target nucleic acid utilized herein can be any nucleic acid, for example, human nucleic acids, bacterial nucleic acids, or viral nucleic acids.
  • a target nucleic acid sample or sample comprising a target nucleic acid can be, for example, a nucleic acid sample from one or more biological samples including, but not limited to whole blood, nucleic acids extracted from whole blood, plasma, nucleic acids extracted from plasma, sputum, stool, urine, cheek or nasal swab, cells, tissues, or bodily fluids.
  • Target biological samples can be derived from any source including, but not limited to, eukaryotes, plants, animals, vertebrates, fish, mammals, humans, non-humans, bacteria, microbes, viruses, biological sources, serum, plasma, blood, urine, semen, lymphatic fluid, cerebrospinal fluid, amniotic fluid, biopsies, needle aspiration biopsies, cancers, tumors, tissues, cells, cell lysates, crude cell lysates, tissue lysates, tissue culture cells, buccal swabs, mouthwashes, stool, mummified tissue, forensic sources, autopsies, archeological sources, infections, nosocomial infections, production sources, drug preparations, biological molecule productions, protein preparations, lipid preparations, carbohydrate preparations, inanimate objects, air, soil, sap, metal, fossils, excavated materials, and/or other terrestrial or extra- terrestrial materials and sources.
  • eukaryotes plants, animals, vertebrates, fish, mammals, humans,
  • the sample may also contain mixtures of material from one source or different sources.
  • nucleic acids of an infecting bacterium or virus can be amplified along with human nucleic acids when nucleic acids from such infected cells or tissues are amplified using the disclosed methods.
  • Types of useful target samples include eukaryotic samples, plant samples, animal samples, vertebrate samples, fish samples, mammalian samples, human samples, non-human samples, bacterial samples, microbial samples, viral samples, biological samples, serum samples, plasma samples, blood samples, urine samples, semen samples, lymphatic fluid samples, cerebrospinal fluid samples, amniotic fluid samples, biopsy samples, needle aspiration biopsy samples, cancer samples, tumor samples, tissue samples, cell samples, cell lysate samples, crude cell lysate samples, tissue lysate samples, tissue culture cell samples, buccal swab samples, mouthwash samples, stool samples, mummified tissue samples, autopsy samples, archeological samples, infection samples, nosocomial infection samples, production samples, drug preparation samples, biological molecule production samples, protein preparation samples, lipid preparation samples, carbohydrate preparation samples, inanimate object samples, air samples, soil samples, sap samples, metal samples, fossil samples, excavated material samples, and/or other terrestrial or extra-terrestrial samples.
  • a target nucleic acid molecule of interest is about 19 to about 1,000,000 nucleotides (nt) in length. In some instances, the target is about 19 to about 100, about 100 to about 1000, about 1000 to about 10,000, about 10,000 to about 100,000, or about 100,000 to about 1,000,000 nucleotides in length.
  • the target is about 20, about 100, about 200, about 300, about 400, about 500, about 600, about 700, about 800, about 900, about 1,000, about 2,000, about 3,000, about 4,000, about 5,000, about 6,000, about 7,000, about 8,000, about 9000, about 10,000, about 20,000, about 30,000, about 40,000, about 50,000, about 60,000, about 70,000, about 80,000, about 90,000, about 100,000, about 200,000, about 300,000, about 400,000, about 500,000, about 600,000, about 700,000, about 800,000, about 900,000, or about 1,000,000 nucleotides in length.
  • the target nucleic acid may be provided in the context of a longer nucleic acid (e.g., such as a coding sequence or gene within a chromosome or a chromosome fragment).
  • a target of interest is linear, while in other instances, a target is circular (e.g., plasmid DNA, mitochondrial DNA, or plastid DNA).
  • a primer-target system comprises one or more nucleic acid targets, a polymerase, and one or more primers (e.g., primer duplex).
  • primer encompasses any one of the primers or primer systems described herein.
  • the primer- target systems described herein comprise a plurality of different primers.
  • a primer-target system can comprise at least two primers, which can be used to identify and, for example amplify, a target nucleic acid molecule.
  • a target nucleic acid molecule may be present amongst a plurality of non-target nucleic acid molecules, for example, as a single copy or in low copy number.
  • Any one of the primer-target systems described herein may comprises conditions similar to those used in nucleic acid amplification or sequencing reactions (e.g., similar reagents, reaction temperature, etc.).
  • kits comprising (1) at least one complement strand having a target-homologous-complementary region (region 2), a target-nonhomologous-complementary region (region 3), and a target-toehold-complementary region (region 1), and (2) at least one protector strand having a target-homologous region (region 4) and a target-nonhomologous region (region 5).
  • kits comprising at least one primer duplex comprising (1) at least one complement strand having a target-homologous-complementary region, a target- nonhomologous-complementary region, and a target-toehold-complementary region, and (2) at least one protector strand having a target-homologous region and a target-nonhomologous region.
  • any one of the kits described herein may further comprise a polymerase, including reverse transcriptase.
  • Any one of the kits provided herein may further comprise one or more agent selected from buffer (e.g., KC1, MgC12, Tris-HCl), dNTPs (e.g., dATP, dCTP, dGTP, dTTP), and water.
  • Any one of the kits provided herein may comprise protector strand is molar excess of the primer.
  • Any one of the kits provided herein may further comprise instructions or directions for obtaining instructions (e.g., from a website) for using the components of the kits.
  • Any one of the kits provided herein may further comprise at least one reaction tube, well, chamber, or the like.
  • compositions of the invention can be used to achieve the methods of the invention.
  • the term "about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among the study subjects.
  • Example 11 furthermore shows the design of a probe intended to operate in a concentration of the denaturant formamide. Also given are the stoichiometric ratios [P]o/[C]o needed to satisfy the standard free energy value of Expression 1 being equal to the standard free energy value of Expression 2.
  • Table 4 Standard free energy and stoichiometric data for the probes of Examples 1-12.
  • Example 1 provides a probe directed to the target nucleic acid BRAF 11-30 as shown in FIG. 9.
  • the following AG° values for hybridization of the probe to the target at 37°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG°V_ T C
  • the stoichiometric ratio ([P]o/[C]o) that allows the value provided by the G 0 ⁇ according to Expression 1 to have value identical to that provided by Expression 2 is also provided in Table 4.
  • the X value provides for the variation in Expression 2 to obtain a value equal to Expression 1 given the corresponding stoichiometric ratios and was 0.00, 1.42, and -1.27 kcal/mol, respectively.
  • Example 2 provides a probe directed to the target nucleic acid BRAF 71-90 as shown in FIG. 10.
  • the following AG° values for hybridization of the probe to the target at 37°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG°V_ T
  • Example 3 provides a probe directed to the target nucleic acid BRAF 131-160 as shown in FIG. 11.
  • the following AG° values for hybridization of the probe to the target at 37°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° nh -pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG° V _
  • Example 4 provides a probe directed to the target nucleic acid BRAF 191-220 as shown in FIG. 12.
  • the following AG° values for hybridization of the probe to the target at 52°C, 1M Na are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AG° V _ T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG° V
  • Example 5 provides a probe directed to the target nucleic acid BRAF 251-280 as shown in FIG. 13.
  • the following AG° values for hybridization of the probe to the target at 65°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n -pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG° V _ T C
  • Example 6 provides a probe directed to the target nucleic acid BRAF 311-350 as shown in FIG. 14.
  • the following AG° values for hybridization of the probe to the target at 52°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n _pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG 0 t _ T c); and (5) AG°TM which is AG 0 t _ T c - AG° NH - P C + (AG° V _ T
  • Example 7 provides a probe directed to the target nucleic acid BRAF 431-460 as shown in FIG. 15.
  • the following AG° values for hybridization of the probe to the target at 65°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG° V _ T
  • Example 8 provides a probe directed to the target nucleic acid BRAF 491-520 as shown in FIG. 16.
  • the following AG° values for hybridization of the probe to the target at 37°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV T C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AGVV P C); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t -Tc - AG° NH - P C + (AG° V _ T C - AG
  • Example 9 provides a probe directed to the target nucleic acid BRAF 551-580 as shown in FIG. 17.
  • the following AG° values for hybridization of the probe to the target at 37°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AG° V _ T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG°
  • Example 10 provides a probe directed to the target nucleic acid BRAF 611-630 as shown in FIG. 18.
  • the following AG° values for hybridization of the probe to the target at 25°C, 1M Na + are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG° t _ T c); and (5) AG 0 TM which is AG° t _ T c - AG° NH - P C + (AG° V _
  • Example 11 provides a probe directed to the target nucleic acid BRAF 670-700 as shown in FIG. 19.
  • the following AG° values for hybridization of the probe to the target at 25°C, 1M Na + in 30% formamide are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target-homologous complementary region 2 of complement strand C to target- validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG 0 t - T c); and (5) AG 0 TM which is AG°t-Tc - + (AGVTC - AG PC) (Expression
  • Example 12 provides a probe directed to a DNA target nucleic acid as shown in FIG. 20.
  • the following AG° values for hybridization of the probe to the target at 62°C, 3 mM Mg 2+ are provided in Table 4 : (1) hybridization of target homologous complementary region 2 of complement strand C to target homologous region 4 of protector strand P (AGV P C); (2) hybridization of target-nonhomologous-complementary region 3 of complement strand C to target-nonhomologous region 5 of protect strand P (AG° n h-pc); (3) hybridization of target- homologous complementary region 2 of complement strand C to target-validation region 7 of target T (AGV T C); (4) hybridization of target-toehold-complementary region 1 of complement strand C to target-toehold region 6 of target T (AG 0 t _ T c); and (5) AG 0 TM which is AG 0 t _ T c - AG° NH - P C + (AG

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Abstract

L'invention concerne des compositions et des procédés pour des sondes et des amorces d'acide nucléique très spécifiques. Le système de sonde comprend un brin complémentaire et un brin protecteur qui forment une sonde partiellement double brin. L'énergie libre standard de réaction de l'hybridation entre la sonde et l'acide nucléique cible, telle que déterminée par l'expression 1 (ΔGo rxn = ΔGo t-TC - ΔGo nh-PC + (ΔGo v-TC - ΔGo h-PC)), est comprise entre environ -4 kcal/mole et environ +4 kcal/mole. En variante, l'énergie libre standard de réaction de l'hybridation entre la sonde et l'acide nucléique cible est déterminée par l'expression 1 comme étant à moins de 5 kcal/mole de l'énergie libre standard telle que déterminée par l'expression 2 (-Rζln(([P]0 - [C]0)/[C]0)]), où le terme [P]0 de l'expression 2 est égal à la concentration du brin protecteur et le terme [C]0 de l'expression 2 est égal à la concentration du brin complémentaire. L'invention concerne, en outre, un procédé pour le réglage fin à la volée, d'une réaction au moyen de la présente sonde.
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WO2017193025A1 (fr) * 2016-05-06 2017-11-09 William Marsh Rice University Purification stoechiométrique d'acide nucléique à l'aide de bibliothèques de sondes de capture à base de randomères
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AU2021294360A1 (en) * 2020-06-26 2023-02-02 William Marsh Rice University Amplicon Comprehensive Enrichment
CN113652469B (zh) * 2021-08-17 2024-08-02 上海市肺科医院 一种去除样本中核糖体rna和/或线粒体rna的方法和试剂盒

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US20210230691A1 (en) 2021-07-29
CN106103818A (zh) 2016-11-09
US10900079B2 (en) 2021-01-26
CA3176365A1 (fr) 2015-06-25
KR102242192B1 (ko) 2021-04-20
CA2934226C (fr) 2022-12-06
JP6637423B2 (ja) 2020-01-29
ES2771773T3 (es) 2020-07-07
JP2016539650A (ja) 2016-12-22
KR20160093687A (ko) 2016-08-08
EP3084051B1 (fr) 2020-01-01
WO2015094429A1 (fr) 2015-06-25
US20160340727A1 (en) 2016-11-24
CA2934226A1 (fr) 2015-06-25

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